Varicella
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Sign up freeTop drugs studied for this disease
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FDA approval · 2021-05-19FDA Approved: ACYCLOVIR — Original Application (Macleods Pharmaceuticals Limited)
FDA approved the original ANDA for acyclovir from Macleods Pharmaceuticals Limited, enabling a generic version of acyclovir to enter the mar…
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CLINICAL_TRIALS trial_result · 2021-04-06Clinical Trial Update: Evaluation of the Immunogenicity and Safety of VARIVAX™ in Healthy Russians (V210-058) [Phase 3]
Phase 3 clinical trial evaluating immunogenicity and safety of VARIVAX in healthy Russian participants has completed with posted results.
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FDA approval · 2020-12-23FDA Approved: ACYCLOVIR — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
The FDA approved a supplemental application for acyclovir submitted by Teva Pharmaceuticals USA, Inc.
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CLINICAL_TRIALS research · 2020-09-18Clinical Trial Update: Immunity Against Varicella in Pediatric Orthotopic Liver Transplantation Recipients [Phase 2, Phase 3]
A pediatric trial update evaluating immunity against varicella in liver transplant recipients undergoing immunosuppression (Phase 2/Phase 3)…
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FDA approval · 2020-07-10FDA Approved: ACYCLOVIR — Original Application (ANI Pharmaceuticals, Inc.)
FDA approved ANI Pharmaceuticals' original ANDA for generic acyclovir (acyclovir). The approval covers treatment of herpes simplex infection…
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FDA approval · 2020-04-23FDA Approved: ACYCLOVIR — Original Application (Chartwell Governmental & Specialty RX, LLC.)
The FDA approved Chartwell Governmental & Specialty RX, LLC.'s generic acyclovir via ANDA 212718, confirming a generic antiviral product. It…
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FDA approval · 2020-03-18FDA Approved: VALACYCLOVIR — Original Application (Westminster Pharmaceuticals, LLC)
FDA approved Westminster Pharmaceuticals' original ANDA for valacyclovir (valacyclovir hydrochloride), a generic antiviral used to treat her…
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CLINICAL_TRIALS trial_result · 2020-03-17Clinical Trial Update: Safety and Immunogenicity of Measles Vaccine, Varicella Vaccine and Hepatitis-A Vaccine [Phase 4]
Phase 4 trial update evaluating safety and immunogenicity of measles, varicella, and hepatitis A vaccines.
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FDA approval · 2020-02-28FDA Approved: VALACYCLOVIR — Supplemental Application (SUN PHARMACEUTICAL INDUSTRIES, INC.)
The FDA approved a supplemental application for valacyclovir from Sun Pharmaceutical Industries, Inc., resulting in changes to the product's…
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FDA approval · 2020-01-29FDA Approved: ACYCLOVIR — Original Application (Xiromed, LLC)
FDA approved the original ANDA for acyclovir from Xiromed, LLC, providing a generic version of the antiviral for herpes simplex virus infect…
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CLINICAL_TRIALS trial_result · 2019-11-15Clinical Trial Update: Study to Evaluate Frozen Versus Refrigerated MMRV (Combined Measles, Mumps, Rubella, and Varicella) Investigational Vaccine (V221-016) [Phase 3]
Phase 3 study comparing frozen versus refrigerated MMRV vaccine (V221-016) completed.
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FDA approval · 2019-10-07FDA Approved: ACYCLOVIR — Original Application (Bionpharma Inc.)
FDA approved the original ANDA for acyclovir by Bionpharma Inc., authorizing a generic version.
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CLINICAL_TRIALS trial_result · 2019-09-23Clinical Trial Update: Evaluate Vaccine Against Chickenpox and a Combined Vaccine Against 4 Viral Childhood Diseases: Measles, Mumps, Rubella and Chickenpox [Phase 3]
Phase 3 trial evaluating a varicella vaccine and a combined Measles, Mumps, Rubella, and Varicella vaccine by GlaxoSmithKline has completed,…
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CLINICAL_TRIALS trial_result · 2019-08-26Clinical Trial Update: Evaluation of Immunogenicity and Safety of VARIVAX® Passage Extension 34 (PE34) Process in Children (V210-A03) [Phase 3]
Phase 3 trial evaluating immunogenicity and safety of the VARIVAX PE34 process in children with varicella; results posted after completion.
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CLINICAL_TRIALS trial_result · 2019-05-08Clinical Trial Update: Immunogenicity and Safety of NBP608 Compared to Varivax in Healthy Children 12 Months to 12 Years of Age [Phase 3]
Phase 3 trial updating immunogenicity and safety of NBP608 compared to Varivax in healthy children aged 12 months to 12 years with varicella…
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FDA approval · 2019-03-15FDA Approved: ACYCLOVIR — Original Application (Viona Pharmaceuticals Inc)
FDA approved the generic acyclovir product from Viona Pharmaceuticals Inc under an Original Application.
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CLINICAL_TRIALS trial_result · 2019-02-04Clinical Trial Update: Detection and Characterisation of Varicella Zoster Virus From Dermal Lesions of Chickenpox-infected Patients [Phase 3]
A Phase 3 trial update from GlaxoSmithKline reports results on detecting and characterising Varicella Zoster Virus from dermal lesions in pa…
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CLINICAL_TRIALS trial_result · 2019-01-18Clinical Trial Update: Safety,Tolerability and Immunogenicity of Vaccination With VARIVAX in Healthy Indian Children (V210-056) [Phase 3]
A Phase 3 study evaluating the safety, tolerability, and immunogenicity of the VARIVAX varicella vaccine in healthy Indian children.
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FDA approval · 2019-01-11FDA Approved: ACYCLOVIR — Original Application (Torrent Pharmaceuticals Limited)
FDA approves Torrent Pharmaceuticals Limited's generic acyclovir tablets through an original ANDA.
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FDA approval · 2018-08-31FDA Approved: ACYCLOVIR — Original Application (Zydus Pharmaceuticals (USA) Inc.)
FDA approved the original application for acyclovir from Zydus Pharmaceuticals (USA) Inc., enabling a generic version of acyclovir.
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CLINICAL_TRIALS trial_result · 2018-08-13Clinical Trial Update: ProQuad® Intramuscular vs Subcutaneous [Phase 3]
Phase 3 trial comparing ProQuad intramuscular vs subcutaneous administration in measles/mumps rubella/varicella indications; results posted …
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CLINICAL_TRIALS trial_result · 2018-06-13Clinical Trial Update: A Phase 3 Lot-consistency Clinical Trial of Live Attenuated Varicella Vaccine [Phase 3]
A Phase 3 lot-consistency trial of a live attenuated varicella vaccine developed by Sinovac has completed.
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CLINICAL_TRIALS withdrawal · 2018-05-09Clinical Trial Update: Response and Clearance of Viral DNA Following Administration of Live Attenuated Varicella Vaccine.
A clinical trial evaluating the response and clearance of Varicella DNA after administration of a live attenuated Varicella vaccine in trans…
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FDA approval · 2018-04-06FDA Approved: ACYCLOVIR — Original Application (Alembic Pharmaceuticals Inc.)
FDA approves Alembic Pharmaceuticals Inc.'s original ANDA for acyclovir, granting a generic version of the antiviral for herpes simplex infe…
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CLINICAL_TRIALS trial_result · 2018-03-19Clinical Trial Update: Immunogenicity and Safety Study of Proquad® and Infanrix® Hexa When Administered Concomitantly (V221-035) [Phase 3]
Phase 3 immunogenicity and safety study assessing concomitant administration of ProQuad and Infanrix Hexa has been completed and results pos…